EP1153040A1 - Procede pour produire des ethers cellulosiques hydrosolubles a basse viscosite - Google Patents
Procede pour produire des ethers cellulosiques hydrosolubles a basse viscositeInfo
- Publication number
- EP1153040A1 EP1153040A1 EP99957311A EP99957311A EP1153040A1 EP 1153040 A1 EP1153040 A1 EP 1153040A1 EP 99957311 A EP99957311 A EP 99957311A EP 99957311 A EP99957311 A EP 99957311A EP 1153040 A1 EP1153040 A1 EP 1153040A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- cellulose
- hydrogen peroxide
- viscosity
- water
- mixture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
- C08B11/20—Post-etherification treatments of chemical or physical type, e.g. mixed etherification in two steps, including purification
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
- C08B11/02—Alkyl or cycloalkyl ethers
- C08B11/04—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals
- C08B11/08—Alkyl or cycloalkyl ethers with substituted hydrocarbon radicals with hydroxylated hydrocarbon radicals; Esters, ethers, or acetals thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
- C08B11/193—Mixed ethers, i.e. ethers with two or more different etherifying groups
Definitions
- cellulose ethers strongly depend on the viscosity of their solutions. While mainly medium viscosity cellulose ethers, i.e. those with a medium molecular weight are processed, but high and low viscosity cellulose ethers have also become important.
- Low-viscosity cellulose ethers which also have a low molecular weight compared to medium- and high-viscosity cellulose ethers, can basically be produced in two different ways. Either one starts from a low molecular weight alkahcellulose and etherifies it, or one degrades a finished cellulose ether up to the desired molecular weight.
- the degradation of high molecular weight cellulose ethers to low molecular weight, low viscosity cellulose ethers mentioned as the second possible method can be caused by the action of oxidizing agents, e.g. Hypochlorite or hydrogen peroxide.
- oxidizing agents e.g. Hypochlorite or hydrogen peroxide.
- the oxidative degradation of higher-viscosity cellulose ethers can be carried out after the cleaning process. Losing losses and difficulties during washing are thus avoided.
- DE 1 543 116 from Kalle AG claims a process for producing low-viscosity cellulose ethers by oxidative degradation of higher-viscosity cellulose ethers with hydrogen peroxide.
- This process is characterized in that a higher-viscosity cellulose ether is mixed with an aqueous solution of hydrogen peroxide, the water content of the mixture not exceeding 75% by weight, based on the total amount.
- the mixture is then dried at temperatures from 100 ° C. to 250 ° C. until the hydrogen peroxide is consumed. The loss of moisture and hydrogen peroxide run almost parallel to the decrease in viscosity.
- the object was to provide a process which allows the viscosity to be adjusted directly after washing the cellulose ether in such a way that the subsequent drying, shaping (grinding, granulation) and mixing are not influenced, and that the degradation reaction is not affected by the subsequent process steps of drying , Shaping (grinding, granulation) and mixing is influenced.
- the mixture is then kept in motion at temperatures of 65-125 ° C., preferably 75-100 ° C. until the hydrogen peroxide is consumed and then dried.
- a low-viscosity, water-soluble cellulose ether is obtained by these processes.
- the subsequent process steps for the production of the ready-to-sell cellulose ether such as drying, shaping (grinding, granulation) and mixing, are not influenced by the degradation reaction.
- the degree of moisture and grinding can be set independently of the reduction in viscosity.
- Low-viscosity cellulose ethers are to be understood here as cellulose ethers whose 2% strength aqueous solutions at 20 ° C. and a shear rate of 2.55 s _ 1 have viscosities of 2 to 400, in particular 2 to 100 mPa * s (Haake Rotovisko).
- a higher-viscosity cellulose ether is to be understood here to mean a cellulose ether whose 2% aqueous solutions at 20 ° C.
- a shear rate of 2.55 s -1 have a viscosity of 100 to 100,000, preferably 400 to 20,000 mPa * s the viscosity reduction in the end product caused by the process according to the invention compared to the starting material is preferably at least 50%, in particular at least 70% and very particularly preferably at least 98%.
- Ionic or nonionic cellulose ethers can be used as the starting material, such as preferably carboxymethyl cellulose, hydrophobically modified carboxymethyl cellulose, hydroxyethyl carboxymethyl cellulose, sulfoethyl cellulose, hydrophobically modified sulfoethyl cellulose, hydroxyethyl sulfoethyl cellulose, hydrophobically modified hydroxyethylsulfoethyl cellulose, hydroxyethyl cellulose, methyl methyl cellulose, methyl methyl cellulose, hydrophobethyl cellulose, - se, methyl hydroxypropyl cellulose, hydroxypropyl cellulose and mixtures or
- Methylhydroxy- are particularly preferred as starting material.
- Water-moist filter cakes of these cellulose ethers, as are present after washing and separation, are advantageously used.
- the process can be conveniently integrated into the usual production flow of a manufacturing process
- Cellulose ether are inserted. After washing, the higher-viscosity starting material is spun off to a dry content of 25 to 80% by weight, based on the total weight.
- An aqueous solution of hydrogen peroxide is then mixed in intensively at temperatures of 65-125 ° C., if appropriate in stages, the mixing ratio being chosen so that the hydrogen peroxide content, based on the dry substance, is 0J-10% by weight , the dry content of the mixture does not fall below 25% by weight, based on the total amount.
- the mixture is then kept at temperatures of 65-125 ° C., preferably temperatures of 75-
- a higher molecular weight cellulose ether with a dry content of 35-80% by weight, particularly preferably 40-55% by weight, based on the total amount, is preferably used in the process.
- 0J to 10% by weight of hydrogen peroxide, based on the dry cellulose ether, are used to degrade the higher-viscosity cellulose ether; preference is given to 0J to 2.5% by weight, particularly preferably 0.5 to 1.8% by weight.
- Hydrogen peroxide, based on the dry cellulose ether work.
- the degradation reaction results in products whose 2% by weight aqueous solutions have acidic pH values of 3 to 5. It has proven to be useful here to adjust the pH of the products before, during or after the degradation reaction, but in any case before each further processing step such as drying or shaping. Particularly good results are achieved if the pH is adjusted after the degradation reaction.
- the pH is adjusted using aqueous solutions of salts which have a pH of 5 to 12 and which may contain all or part of the hydrogen peroxide required. These solutions are added to the reaction mixture in such quantities that the pH
- the value of the mixture after the addition is set to greater than 4.5, preferably to 6 to 7.
- Aqueous solutions of sodium dihydrogen phosphate, disodium hydrogen phosphate, trisodium phosphate, disodium carbonate and sodium bicarbonate or aqueous solutions of mixtures of these salts are advantageously used.
- alkali salts of weak acids such as those of
- Citric acid or succinic acid can be used in the form of aqueous buffer solutions.
- An advantage of the claimed method is that the actual molecular weight reduction is completely decoupled from subsequent drying.
- any drying units with different residence time behavior of the cellulose ether particles to be dried can be used without having an influence on the degradation reaction.
- only one unit, the mixer in which the degradation reaction is carried out is affected by the corrosive properties of the hydrogen peroxide introduced.
- additives and modifiers after the degradation reaction, but before drying in the solvent-moist (eg water-moist) cellulose ether.
- the group of dialdehydes should be mentioned here in particular. These compounds are used for the production of solution-delayed cellulose ethers. Their use together with the hydrogen peroxide required for the degradation reaction is prohibited due to their oxidation possibility. It is also possible to mix in oligomeric or polymeric substances sensitive to oxidation (eg polysaccharides, polysaccharide ethers, polyvinyl alcohol, polyesters, polyamides) after the degradation reaction and before drying.
- the amount of hydrogen peroxide used, the initial viscosity and the final viscosity can be found in the table.
- the amounts given relate to the dry methylhydroxyethyl cellulose.
- Amounts of disodium hydrogen phosphate and disodium carbonate, as well as the pH values of 2% by weight solutions of the products and the hydrogen peroxide used quantity can be found in the table.
- the amounts given relate to the dry methylhydroxyethyl cellulose.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DK99957311T DK1153040T3 (da) | 1998-11-27 | 1999-11-15 | Fremgangsmåde til fremstilling af vandoplöselige celluloseethere med lav viskositet |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19854770 | 1998-11-27 | ||
DE19854770A DE19854770A1 (de) | 1998-11-27 | 1998-11-27 | Verfahren zur Herstellung niedrigviskoser wasserlöslicher Celluloseether |
PCT/EP1999/008779 WO2000032636A1 (fr) | 1998-11-27 | 1999-11-15 | Procede pour produire des ethers cellulosiques hydrosolubles a basse viscosite |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1153040A1 true EP1153040A1 (fr) | 2001-11-14 |
EP1153040B1 EP1153040B1 (fr) | 2005-06-08 |
Family
ID=7889225
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP99957311A Revoked EP1153040B1 (fr) | 1998-11-27 | 1999-11-15 | Procede pour produire des ethers cellulosiques hydrosolubles a basse viscosite |
Country Status (17)
Country | Link |
---|---|
US (1) | US6939961B1 (fr) |
EP (1) | EP1153040B1 (fr) |
JP (1) | JP2002531593A (fr) |
KR (1) | KR20010080592A (fr) |
CN (1) | CN1269841C (fr) |
AT (1) | ATE297411T1 (fr) |
AU (1) | AU1506100A (fr) |
BR (1) | BR9915690A (fr) |
CA (1) | CA2352186C (fr) |
DE (2) | DE19854770A1 (fr) |
ES (1) | ES2242432T3 (fr) |
HK (1) | HK1044005B (fr) |
NO (1) | NO20012577D0 (fr) |
PL (1) | PL349790A1 (fr) |
TR (1) | TR200101448T2 (fr) |
UA (1) | UA73294C2 (fr) |
WO (1) | WO2000032636A1 (fr) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006507373A (ja) * | 2002-07-10 | 2006-03-02 | アクゾ ノーベル ナムローゼ フェンノートシャップ | 水溶性ポリサッカライドの脱重合 |
JP3905833B2 (ja) * | 2002-12-27 | 2007-04-18 | 伊那食品工業株式会社 | 増粘用添加物 |
CN102276732B (zh) | 2003-11-28 | 2016-01-20 | 伊士曼化工公司 | 纤维素共聚体和氧化方法 |
WO2009061815A1 (fr) * | 2007-11-09 | 2009-05-14 | Union Carbide Chemicals & Plastics Technology Llc | Procédé de préparation d'un éther de cellulose à très faible viscosité et produit qui en résulte |
US9512237B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Method for inhibiting the growth of microbes with a modified cellulose fiber |
US9512563B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Surface treated modified cellulose from chemical kraft fiber and methods of making and using same |
KR101805048B1 (ko) | 2009-05-28 | 2017-12-05 | 게페 첼루로제 게엠베하 | 화학적 크래프트 섬유로부터의 변형된 셀룰로즈 및 이들을 제조 및 사용하는 방법 |
US9511167B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
SI2505615T1 (sl) * | 2011-04-01 | 2014-08-29 | Omya International Ag | Samovezujoäśi pigmentni hibrid |
SI2662418T1 (sl) | 2012-05-11 | 2015-05-29 | Omya International Ag | Stabilni sprejemljivi polimeri |
KR101971738B1 (ko) * | 2012-12-11 | 2019-04-23 | 롯데정밀화학 주식회사 | 부분 중화법을 통한 초저점도 히드록시알킬 셀룰로오스의 제조방법 |
KR102033179B1 (ko) * | 2012-12-28 | 2019-10-16 | 롯데정밀화학 주식회사 | 스킴코트 모르타르용 첨가제 및 이를 포함하는 스킴코트 모르타르 조성물 |
KR101586136B1 (ko) * | 2013-01-09 | 2016-01-15 | 신에쓰 가가꾸 고교 가부시끼가이샤 | 저중합도 셀룰로오스에테르의 제조 방법 및 이에 따라 제조된 셀룰로오스에테르 |
WO2014140940A2 (fr) | 2013-03-15 | 2014-09-18 | Gp Cellulose Gmbh | Fibre kraft à faible viscosité ayant une teneur en carboxyle améliorée et procédés de production et d'utilisation de celle-ci |
CN104558203B (zh) * | 2015-01-22 | 2016-08-24 | 湖州展望药业股份有限公司 | 一种特低粘度高取代羟丙基纤维素醚的制备方法及其制品 |
KR102373750B1 (ko) * | 2016-10-06 | 2022-03-15 | 신에쓰 가가꾸 고교 가부시끼가이샤 | 저중합도 셀룰로오스 에테르의 제조 방법 |
DE102017223690A1 (de) * | 2017-12-22 | 2019-06-27 | Se Tylose Gmbh & Co. Kg | Oxidativer Abbau von Celluloseethern |
CN109336983B (zh) * | 2018-11-15 | 2020-12-29 | 泸州北方纤维素有限公司 | 用于特低粘羟乙基纤维素的制备方法 |
CN109627346A (zh) * | 2018-12-06 | 2019-04-16 | 泸州北方纤维素有限公司 | 稳定性良好的超低粘度乙基纤维素及其制备方法 |
CN113683470A (zh) * | 2021-08-23 | 2021-11-23 | 姚鲁 | 一种改善射钉装药制造的安全和环保方法 |
CN115572107B (zh) * | 2022-11-11 | 2024-01-19 | 亚士创能新材料(滁州)有限公司 | 耐温变施工的真石漆及其制备方法、应用 |
Family Cites Families (14)
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GB953944A (en) * | 1962-02-16 | 1964-04-02 | Ici Ltd | Reduction of viscosity of water-soluble non-ionic cellulose ethers |
DE1543116A1 (de) * | 1965-05-29 | 1969-07-31 | Kalle Ag | Verfahren zur Herstellung niedrigviskoser wasserloeslicher Celluloseaether |
US3728331A (en) * | 1969-04-04 | 1973-04-17 | Dow Chemical Co | Process for reducing the viscosity of a cellulose ether with hydrogen peroxide |
JPS5928321B2 (ja) * | 1979-02-16 | 1984-07-12 | 株式会社興人 | カルボキシメチルセルロ−スのマ−セル化方法 |
JPS5941643B2 (ja) * | 1979-02-15 | 1984-10-08 | 株式会社興人 | 低粘度カルボキシメチルエチルセルロ−スの製造法 |
DE3009149A1 (de) * | 1980-03-10 | 1981-09-24 | Kohjin Co., Ltd., Tokyo | Verfahren zum veraethern von cellulosen |
JPS6051481B2 (ja) * | 1981-04-30 | 1985-11-14 | 株式会社興人 | 低粘度セルロ−スエ−テル類の製造方法 |
DE3839831A1 (de) * | 1988-11-25 | 1990-05-31 | Hoechst Ag | Verfahren und vorrichtung zur produktschonenden mahlung und gleichzeitigen trocknung von feuchten celluloseethern |
JP2800061B2 (ja) * | 1990-05-21 | 1998-09-21 | ダイセル化学工業株式会社 | 低粘度カルボキシメチルセルロースナトリウムの製造法 |
JP2800062B2 (ja) * | 1990-05-21 | 1998-09-21 | ダイセル化学工業株式会社 | 超低粘度カルボキシメチルセルロースナトリウム塩 |
DE69129608T2 (de) * | 1990-07-02 | 1998-10-15 | Aqualon Co | Niedrigviskose-Polysaccharidzusammensetzung mit hohem Festkörpergehalt |
JPH0681761B2 (ja) * | 1991-07-12 | 1994-10-19 | 三洋化成工業株式会社 | セルロース誘導体の低分子化方法および低分子量セルロース誘導体のエーテル化方法 |
GB2262527A (en) * | 1992-07-02 | 1993-06-23 | Dow Deutschland Inc | Process for grinding cellulose compounds |
DE4411681A1 (de) * | 1994-04-05 | 1995-10-12 | Hoechst Ag | Verfahren zur Herstellung niedermolekularer Polysaccharidether |
-
1998
- 1998-11-27 DE DE19854770A patent/DE19854770A1/de not_active Withdrawn
-
1999
- 1999-11-15 BR BR9915690-3A patent/BR9915690A/pt not_active Application Discontinuation
- 1999-11-15 UA UA2001064446A patent/UA73294C2/uk unknown
- 1999-11-15 AU AU15061/00A patent/AU1506100A/en not_active Abandoned
- 1999-11-15 CA CA002352186A patent/CA2352186C/fr not_active Expired - Fee Related
- 1999-11-15 ES ES99957311T patent/ES2242432T3/es not_active Expired - Lifetime
- 1999-11-15 TR TR2001/01448T patent/TR200101448T2/xx unknown
- 1999-11-15 US US09/856,545 patent/US6939961B1/en not_active Expired - Fee Related
- 1999-11-15 JP JP2000585276A patent/JP2002531593A/ja active Pending
- 1999-11-15 AT AT99957311T patent/ATE297411T1/de not_active IP Right Cessation
- 1999-11-15 PL PL99349790A patent/PL349790A1/xx not_active Application Discontinuation
- 1999-11-15 DE DE59912164T patent/DE59912164D1/de not_active Revoked
- 1999-11-15 WO PCT/EP1999/008779 patent/WO2000032636A1/fr not_active Application Discontinuation
- 1999-11-15 KR KR1020017006602A patent/KR20010080592A/ko not_active Application Discontinuation
- 1999-11-15 CN CNB998137154A patent/CN1269841C/zh not_active Expired - Fee Related
- 1999-11-15 EP EP99957311A patent/EP1153040B1/fr not_active Revoked
-
2001
- 2001-05-25 NO NO20012577A patent/NO20012577D0/no not_active Application Discontinuation
-
2002
- 2002-07-23 HK HK02105446.7A patent/HK1044005B/zh not_active IP Right Cessation
Non-Patent Citations (1)
Title |
---|
See references of WO0032636A1 * |
Also Published As
Publication number | Publication date |
---|---|
CN1334822A (zh) | 2002-02-06 |
BR9915690A (pt) | 2001-11-13 |
ATE297411T1 (de) | 2005-06-15 |
TR200101448T2 (tr) | 2002-04-22 |
NO20012577L (no) | 2001-05-25 |
NO20012577D0 (no) | 2001-05-25 |
WO2000032636A1 (fr) | 2000-06-08 |
HK1044005B (zh) | 2007-03-30 |
DE19854770A1 (de) | 2000-05-31 |
ES2242432T3 (es) | 2005-11-01 |
JP2002531593A (ja) | 2002-09-24 |
DE59912164D1 (de) | 2005-07-14 |
CA2352186A1 (fr) | 2000-06-08 |
CN1269841C (zh) | 2006-08-16 |
KR20010080592A (ko) | 2001-08-22 |
UA73294C2 (en) | 2005-07-15 |
CA2352186C (fr) | 2008-12-30 |
PL349790A1 (en) | 2002-09-09 |
HK1044005A1 (en) | 2002-10-04 |
US6939961B1 (en) | 2005-09-06 |
AU1506100A (en) | 2000-06-19 |
EP1153040B1 (fr) | 2005-06-08 |
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